Allele Registry

Canonical Allele Identifier: PA101457

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001056

ClinVar Variation:

1001

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Gly310Asp	CA251659 NM_152778.4:c.929G>A